Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001135597.1 | 6069 | Missense Mutation | CAA,GAA | Q1868E | NP_001129069.1 |
NM_001254943.1 | 6069 | Missense Mutation | CAA,GAA | Q1794E | NP_001241872.1 |
NM_018084.4 | 6069 | Missense Mutation | CAA,GAA | Q1841E | NP_060554.3 |
XM_005264418.4 | 6069 | Intron | XP_005264475.1 | ||
XM_005264421.2 | 6069 | Missense Mutation | CAA,GAA | Q1842E | XP_005264478.1 |
XM_005264426.2 | 6069 | Intron | XP_005264483.1 | ||
XM_011532965.2 | 6069 | Missense Mutation | CAA,GAA | Q1869E | XP_011531267.1 |
XM_011532966.2 | 6069 | Missense Mutation | CAA,GAA | Q1869E | XP_011531268.1 |
XM_011532967.2 | 6069 | Missense Mutation | CAA,GAA | Q1841E | XP_011531269.1 |
XM_011532968.2 | 6069 | Missense Mutation | CAA,GAA | Q1795E | XP_011531270.1 |
XM_017004476.1 | 6069 | Intron | XP_016859965.1 | ||
XM_017004477.1 | 6069 | Intron | XP_016859966.1 | ||
XM_017004478.1 | 6069 | Intron | XP_016859967.1 | ||
XM_017004479.1 | 6069 | Intron | XP_016859968.1 | ||
XM_017004480.1 | 6069 | Intron | XP_016859969.1 | ||
XM_017004481.1 | 6069 | Missense Mutation | CAA,GAA | Q1795E | XP_016859970.1 |